Frequency of loss of hMLH1 expression in colorectal carcinoma increases with advancing age
Open Access
- 3 March 2003
- Vol. 97 (6) , 1421-1427
- https://doi.org/10.1002/cncr.11206
Abstract
BACKGROUND The correlation between age at diagnosis and loss of expression of hMLH1 protein in patients with colorectal carcinoma (CRC) has not been evaluated systematically. METHODS Immunohistochemistry was performed for hMLH1 protein in tumor samples from 867 patients with CRC. The authors defined tumors arising in the cecum, ascending colon, and transverse colon as right-sided and tumors arising in the descending colon, sigmoid colon, and rectum as left-sided. Patients' gender, tumor location (side), and hMLH1 expression were analyzed by age groups. RESULTS The percentage of tumors with hMLH1 expression loss increased significantly with advancing age (P < 0.0001): There were no tumors in patients age < 40 years that manifested loss of hMLH1 expression, compared with 29% of tumors that manifested loss of hMLH1 expression in patients age > 90 years. Loss of hMLH1 expression occurred more often in patients with right-sided tumors (32.7% vs. 5.2% of patients with left-sided tumors; P < 0.0001) and in tumors from female patients (24.3% vs. 11.5% of tumors from male patients; P < 0.0001). There was no evidence of interaction between gender and tumor location. CONCLUSIONS Loss of hMLH1 expression in patients with CRC was associated strongly with increasing age. hMLH1 expression loss was more pronounced in tumors from female patients and in tumors that originated on the right side of the colon. Loss of hMLH1 expression in right-sided tumors occurred in nearly 50% of patients age > 90 years. This age-related trend also was observed for males and in tumors that originated in the left colon. Cancer 2003;97:1421–7. © 2003 American Cancer Society. DOI 10.1002/cncr.11206Keywords
This publication has 26 references indexed in Scilit:
- Replication error phenotype, clinicopathological variables, and patient outcome in Dukes' B stage II (T3,N0,M0) colorectal cancerGut, 2000
- CpG island methylator phenotype in colorectal cancerProceedings of the National Academy of Sciences, 1999
- Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinomaProceedings of the National Academy of Sciences, 1998
- Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis.Proceedings of the National Academy of Sciences, 1996
- Increased cytosine DNA-methyltransferase activity is target-cell-specific and an early event in lung cancer.Proceedings of the National Academy of Sciences, 1996
- Methylation of the oestrogen receptor CpG island links ageing and neoplasia in human colonNature Genetics, 1994
- Mutation of a mutL Homolog in Hereditary Colon CancerScience, 1994
- The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancerCell, 1993
- Microsatellite Instability in Cancer of the Proximal ColonScience, 1993
- Colorectal Cancer: Evidence for Distinct Genetic Categories Based on Proximal or Distal Tumor LocationAnnals of Internal Medicine, 1990